Segregation of a Missense Mutation in the Microtubule-Associated Protein Tau Gene with Familial Frontotemporal Dementia and Parkinsonism-Reference-Cited by-同舟云学术

Segregation of a Missense Mutation in the Microtubule-Associated Protein Tau Gene with Familial Frontotemporal Dementia and Parkinsonism

Published:1998-10-01 Issue:11 Volume:7 Page:1825-1829
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Dumanchin C.,Camuzat A.,Campion D.,Verpillat P.,Hannequin D.,Dubois B.,Saugier-Veber P.,Martin C.,Penet C.,Charbonnier F.,Agid Y.,Frebourg T.,Brice A.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/7/11/1825/6955601/7-11-1825.pdf

Reference22 articles.

1. Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia- parkinsonism-amyotrophy complex

2. Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration

3. Familial Multiple-System Tauopathy with Presenile Dementia Is Localized to Chromosome 17

4. Familial progressive subcortical gliosis: Presence of prions and linkage to chromosome 17

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